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Items: 1 to 20 of 279

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098069copy number variation1nstd102humanPathogenic GRCh37 chr9: 136,501,494-136,505,134 , GRCh38.p12 chr9: 133,636,372-133,640,012 DBH
    nsv7098066copy number variation4nstd102humanUncertain significance GRCh37 chr9: 135,139,626-140,034,216 , GRCh38.p12 chr9: 132,264,239-137,139,764 LINC02692, SNORD141A, 181 more genes
    nsv7097936copy number variation1nstd102humanUncertain significance GRCh37 chr9: 136,501,494-136,523,569 , GRCh38.p12 chr9: 133,636,372-133,658,447 DBH, DBH-AS1
    nsv7097700copy number variation1nstd102humanUncertain significance GRCh37 chr9: 136,501,494-136,501,852 , GRCh38.p12 chr9: 133,636,372-133,636,730 DBH
    nsv7097697copy number variation1nstd102humanUncertain significance GRCh37 chr9: 136,218,768-141,016,451 , GRCh38.p12 chr9: 133,351,913-138,121,999 LOC105376326, LOC107987143, 186 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7075196inversion1nstd229human GRCh38 chr9: 130,990,409-137,053,229 , GRCh37.p13 chr9: 133,865,796-139,947,681 LINC02907, LCN1, 196 more genes
    nsv7061943inversion1nstd229human GRCh38 chr9: 133,651,150-133,651,360 , GRCh37.p13 chr9: 136,516,272-136,516,482 DBH
    nsv7060209inversion1nstd229human GRCh38 chr9: 133,220,670-135,537,297 , GRCh37.p13 chr9: 136,369,193-138,429,143 COL5A1, DBH, 66 more genes
    nsv7059760inversion1nstd229human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 LCN10, RAPGEF1, 196 more genes
    nsv6897104copy number variation1nstd229human GRCh38 chr9: 133,657,330-133,661,308 , GRCh37.p13 chr9: 136,522,452-136,526,430 DBH, DBH-AS1, 1 more genes
    nsv6891914copy number variation1nstd229human GRCh38 chr9: 133,646,639-133,646,685 , GRCh37.p13 chr9: 136,511,761-136,511,807 DBH
    nsv6884502copy number variation1nstd229human GRCh38 chr9: 133,630,771-133,737,768 , GRCh37.p13 chr9: 136,495,893-136,602,890 SARDH, DBH-AS1, 1 more genes
    nsv6883433copy number variation1nstd229human GRCh38 chr9: 133,635,621-133,638,332 , GRCh37.p13 chr9: 136,500,743-136,503,454 DBH
    nsv6879602copy number variation1nstd229human GRCh38 chr9: 133,659,201-133,665,600 , GRCh37.p13 chr9: 136,524,323-136,530,722 SARDH, DBH
    nsv6878863copy number variation1nstd229human GRCh38 chr9: 133,634,686-133,640,045 , GRCh37.p13 chr9: 136,499,808-136,505,167 DBH
    nsv6878227copy number variation1nstd229human GRCh38 chr9: 133,633,176-133,639,342 , GRCh37.p13 chr9: 136,498,298-136,504,464 DBH
    nsv6556944inversion1nstd223human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 MIR4669, AK8, 196 more genes
    nsv6448678copy number variation1nstd223human GRCh38 chr9: 133,647,142-133,647,473 , GRCh37.p13 chr9: 136,512,264-136,512,595 DBH
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